A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1023753



Internal ID19112970
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:126387613..126471673hg38UCSC Ensembl
Innerchr8:127399858..127483918hg19UCSC Ensembl
Innerchr8:127469040..127553100hg18UCSC Ensembl
Cytoband8q24.21
Allele length
AssemblyAllele length
hg3884061
hg1984061
hg1884061
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3691514
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1023753
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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